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Effects of senescent lens epithelial cells on the severity of age-related cortical cataract in humans: A case–control study

The aging of lens progenitor cell has been repeatedly proposed to play a key role in age-related cataracts (ARCs), but the mechanism is far from being understood. The present study aims to investigate the relationship between aging of lens progenitor/epithelial cells and the 4 subtypes of ARCs in hu...

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Autores principales: Fu, Qiuli, Qin, Zhenwei, Yu, Jiexin, Yu, Yinhui, Tang, Qiaomei, Lyu, Danni, Zhang, Lifang, Chen, Zhijian, Yao, Ke
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer Health 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4998311/
https://www.ncbi.nlm.nih.gov/pubmed/27336873
http://dx.doi.org/10.1097/MD.0000000000003869
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author Fu, Qiuli
Qin, Zhenwei
Yu, Jiexin
Yu, Yinhui
Tang, Qiaomei
Lyu, Danni
Zhang, Lifang
Chen, Zhijian
Yao, Ke
author_facet Fu, Qiuli
Qin, Zhenwei
Yu, Jiexin
Yu, Yinhui
Tang, Qiaomei
Lyu, Danni
Zhang, Lifang
Chen, Zhijian
Yao, Ke
author_sort Fu, Qiuli
collection PubMed
description The aging of lens progenitor cell has been repeatedly proposed to play a key role in age-related cataracts (ARCs), but the mechanism is far from being understood. The present study aims to investigate the relationship between aging of lens progenitor/epithelial cells and the 4 subtypes of ARCs in humans. Lens capsules, which were collected from ARC patients during surgery, were divided into 3 groups according to the age of patients (50–60, 60–80, and >80 years). The expressions of lens progenitor cell-related markers Sox2, Abcg2, and Ki67 were first examined in human lens epithelial cells (HLECs) in situ. Then, the percentage of senescent and SA-β-gal(+) HLECs isolated from lens capsules were quantified. Finally, the potential relationships between the percentage of senescent (and SA-β-gal(+)) HLECs and the severity of ARCs were analyzed. Ki67(+), Sox2(+), and Abcg2(+) HLECs in lens capsules were clearly more abundant in young people than in patients older than 50 years, and they were almost absent in patients older than 60 years. The percentage of primary HLECs with aging morphology increased with age, consistent with the results of SA-β-gal(+) primary HLECs. Only cortical cataract classification was found to be strongly related to the percentage of SA-β-gal(+) and senescent HLECs. Our study gave the initial evidence on the dynamical change of lens stem/progenitor cells in human lens capsule with age and suggested that lens progenitor/epithelial cell aging is important in the severity of cortical cataracts.
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spelling pubmed-49983112016-09-02 Effects of senescent lens epithelial cells on the severity of age-related cortical cataract in humans: A case–control study Fu, Qiuli Qin, Zhenwei Yu, Jiexin Yu, Yinhui Tang, Qiaomei Lyu, Danni Zhang, Lifang Chen, Zhijian Yao, Ke Medicine (Baltimore) 5800 The aging of lens progenitor cell has been repeatedly proposed to play a key role in age-related cataracts (ARCs), but the mechanism is far from being understood. The present study aims to investigate the relationship between aging of lens progenitor/epithelial cells and the 4 subtypes of ARCs in humans. Lens capsules, which were collected from ARC patients during surgery, were divided into 3 groups according to the age of patients (50–60, 60–80, and >80 years). The expressions of lens progenitor cell-related markers Sox2, Abcg2, and Ki67 were first examined in human lens epithelial cells (HLECs) in situ. Then, the percentage of senescent and SA-β-gal(+) HLECs isolated from lens capsules were quantified. Finally, the potential relationships between the percentage of senescent (and SA-β-gal(+)) HLECs and the severity of ARCs were analyzed. Ki67(+), Sox2(+), and Abcg2(+) HLECs in lens capsules were clearly more abundant in young people than in patients older than 50 years, and they were almost absent in patients older than 60 years. The percentage of primary HLECs with aging morphology increased with age, consistent with the results of SA-β-gal(+) primary HLECs. Only cortical cataract classification was found to be strongly related to the percentage of SA-β-gal(+) and senescent HLECs. Our study gave the initial evidence on the dynamical change of lens stem/progenitor cells in human lens capsule with age and suggested that lens progenitor/epithelial cell aging is important in the severity of cortical cataracts. Wolters Kluwer Health 2016-06-24 /pmc/articles/PMC4998311/ /pubmed/27336873 http://dx.doi.org/10.1097/MD.0000000000003869 Text en Copyright © 2016 Wolters Kluwer Health, Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial License 4.0 (CCBY-NC), where it is permissible to download, share, remix, transform, and buildup the work provided it is properly cited. The work cannot be used commercially. http://creativecommons.org/licenses/by-nc/4.0
spellingShingle 5800
Fu, Qiuli
Qin, Zhenwei
Yu, Jiexin
Yu, Yinhui
Tang, Qiaomei
Lyu, Danni
Zhang, Lifang
Chen, Zhijian
Yao, Ke
Effects of senescent lens epithelial cells on the severity of age-related cortical cataract in humans: A case–control study
title Effects of senescent lens epithelial cells on the severity of age-related cortical cataract in humans: A case–control study
title_full Effects of senescent lens epithelial cells on the severity of age-related cortical cataract in humans: A case–control study
title_fullStr Effects of senescent lens epithelial cells on the severity of age-related cortical cataract in humans: A case–control study
title_full_unstemmed Effects of senescent lens epithelial cells on the severity of age-related cortical cataract in humans: A case–control study
title_short Effects of senescent lens epithelial cells on the severity of age-related cortical cataract in humans: A case–control study
title_sort effects of senescent lens epithelial cells on the severity of age-related cortical cataract in humans: a case–control study
topic 5800
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4998311/
https://www.ncbi.nlm.nih.gov/pubmed/27336873
http://dx.doi.org/10.1097/MD.0000000000003869
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